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pro vyhledávání: '"genetics [Phosphoinositide Phospholipase C]"'
Autor:
Balendra, Rubika, Uphill, James, Collinson, Claire, Druyeh, Ronald, Adamson, Gary, Hummerich, Holger, Zerr, Inga, Gambetti, Pierluigi, Collinge, John, Mead, Simon
Publikováno v:
BMC medical genetics 17(1), 28 (2016). doi:10.1186/s12881-016-0278-2
BMC Medical Genetics
BMC Medical Genetics
Background Human prion diseases are relentlessly progressive neurodegenerative disorders which include sporadic Creutzfeldt-Jakob disease (sCJD) and variant CJD (vCJD). Aside from variants of the prion protein gene (PRNP) replicated association at ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::9b847810d2af54ab2fd141e3d0be061f
https://pub.dzne.de/record/138482
https://pub.dzne.de/record/138482